# FDA recall D-1177-2017

> **Pfizer Inc.** · Class II · drug recall initiated 2017-09-01.

## Product

Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24

## Reason for recall

Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-1177-2017
- **Recalling firm:** Pfizer Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-09-01
- **Report date:** 2017-10-04
- **Termination date:** 2020-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1177-2017

## Citation

> AI Analytics. FDA recall D-1177-2017. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/D-1177-2017. Source: US FDA. Licensed CC0.

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